A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18209707



Internal ID20776747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:151178849..151449476hg38UCSC Ensembl
chr3:150896636..151167264hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg38270628
hg19270629
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6356250
Supporting Variants
Samples
Known GenesGPR171, GPR87, IGSF10, MED12L, P2RY12, P2RY13, P2RY14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18209707
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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